hemofili hastalığı

listen to the pronunciation of hemofili hastalığı
Türkisch - Englisch
(Tıp) hemophilia
disease in which the blood does not clot properly after an injury The result can be serious internal bleeding It is suffered mainly by males, who inherit it from their mothers
A largely inherited clotting disorder that occurs almost exclusively in males The disorder delays coagulation, making bleeding difficult to control
any of several hereditary blood-coagulation disorders in which the blood fails to clot normally because of a deficiency or an abnormality of one of the clotting factors; hemophilia, a recessive trait associated with the X-chromosome, is manifested almost exclusively in males
congenital tendency to uncontrolled bleeding; usually affects males and is transmitted from mother to son
An inherited disease that affects mostly males and prevents normal blood clotting It is treated by lifelong injections of a synthetic version of the clotting factor lacking in persons with the disease
{i} hereditary disorder characterized by a failure of the blood to clot normally
Term describing the condition in which patients have an abnormal tendency to bleed because they are unable to adequately form clots
an inherited bleeding disorder caused by low levels, or absence of, a blood protein that is essential for clotting; hemophilia A is caused by a lack of the blood clotting protein factor VIII; hemophilia B is caused by a deficiency of factor IX
see haemophilia. the American spelling of haemophilia (hemo- + -philia). Hereditary bleeding disorder caused by deficiency of a coagulation factor. Lack of factor VIII causes classic hemophilia; other types are caused by deficiency of factor IX or XI. The first two are transmitted by sex-linked heredity; the third has dominant inheritance and occurs in females as well as males. Spontaneous bleeding may occur. Even trivial injury can cause life-threatening blood loss. Drugs can be given to stop bleeding. Heavy blood loss requires blood transfusions
An inherited deficiency in blood-clotting ability, which can cause serious internal bleeding
familial disease appearing in males, transmitted by females, characterized by absence of specific globulin in blood and imperfect coagulation
An inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhages spontaneous or traumatic, because of the result of a missing or a low amount of one of the clotting factors
An X-linked recessive genetic disease, caused by a mutation in the gene for clotting factor VIII (hemophilia A) or clotting factor IX (hemophilia B), which leads to abnormal blood clotting
hemofili hastalığı
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